These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

239 related items for PubMed ID: 6818487

  • 1. Vacuolar myopathy with type 2 A fiber atrophy and type 2 B fiber deficiency. A case of childhood form acid alpha-1,4-glucosidase deficiency.
    Matsuishi T, Terasawa K, Yoshida I, Yano E, Yamashita F, Hidaka T, Ishihara O, Yoshino M, Nonaka I, Kurokawa T, Nakamura Y.
    Neuropediatrics; 1982 Nov; 13(4):173-6. PubMed ID: 6818487
    [Abstract] [Full Text] [Related]

  • 2. [Childhood acid maltase deficiency. A case report].
    Higashi Y, Shirabe T, Yasuda T, Inoue S, Sawayama T.
    Rinsho Shinkeigaku; 1988 Jan; 28(1):83-91. PubMed ID: 3133150
    [No Abstract] [Full Text] [Related]

  • 3. Infantile acid maltase deficiency. II. Muscle fiber hypertrophy and the ultrastructure of end-stage fibers.
    Griffin JL.
    Virchows Arch B Cell Pathol Incl Mol Pathol; 1984 Jan; 45(1):37-50. PubMed ID: 6199886
    [Abstract] [Full Text] [Related]

  • 4. Infantile-acute acid maltase deficiency (Pompe's disease): studies of muscle cultures.
    Meola G, Scarpini E, Manfredi L, Velicogna M, Pellegrini G, Redi CA, Scarlato G.
    Basic Appl Histochem; 1984 Jan; 28(3):245-55. PubMed ID: 6440527
    [Abstract] [Full Text] [Related]

  • 5. [Muscle type acid maltase deficiency. An intermediate case between childhood type and adult type (author's transl)].
    Nakagawa M, Nakazato O, Osame M, Nakashima H, Igata A.
    Rinsho Shinkeigaku; 1982 Jan; 22(1):57-65. PubMed ID: 6807597
    [No Abstract] [Full Text] [Related]

  • 6. Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 36-1986. A 29-year-old woman with slowly progressive proximal-muscle weakness.
    N Engl J Med; 1986 Sep 11; 315(11):694-701. PubMed ID: 3092049
    [No Abstract] [Full Text] [Related]

  • 7. Comparative investigation of alpha-glucosidase activity in leucocytes and skeletal muscle of patients with Morbus Pompe.
    Didt L, Winkler M, Bührdel P, Bormann M, Böhme HJ, Hofmann E.
    Z Med Lab Diagn; 1988 Sep 11; 29(1):7-11. PubMed ID: 3129881
    [No Abstract] [Full Text] [Related]

  • 8. [Acid maltase deficiency myopathy infantile and adult forms (author's transl)].
    Saenz Lope E, Cocero Oviedo E, Ricoy Campo JR, Benlloch T.
    Arch Neurobiol (Madr); 1981 Sep 11; 44(1):49-62. PubMed ID: 6784694
    [No Abstract] [Full Text] [Related]

  • 9. [Hepatic involvement in a case of lysosomal glycogen storage disease with normal acid maltase].
    Matsumoto S, Yamada T, Tanaka K, Hara H, Nonaka I, Uchida T, Miyagi Y, Fukutomi T, Kira J.
    Rinsho Shinkeigaku; 1999 Jul 11; 39(7):717-21. PubMed ID: 10548908
    [Abstract] [Full Text] [Related]

  • 10. Nosology of lysosomal glycogen storage diseases without in vitro acid maltase deficiency. Delineation of a neonatal form.
    Verloes A, Massin M, Lombet J, Grattagliano B, Soyeur D, Rigo J, Koulischer L, Van Hoof F.
    Am J Med Genet; 1997 Oct 17; 72(2):135-42. PubMed ID: 9382133
    [Abstract] [Full Text] [Related]

  • 11. Infantile acid maltase deficiency. III. Ultrastructure of metachromatic material and glycogen in muscle fibers.
    Griffin JL.
    Virchows Arch B Cell Pathol Incl Mol Pathol; 1984 Oct 17; 45(1):51-61. PubMed ID: 6199887
    [Abstract] [Full Text] [Related]

  • 12. [Acid maltase deficiency in 2 adolescent siblings].
    Gracia P, Benlloch T, de la Fuente G, Durántez A, Espanña P, Cánovas A, Illera ER.
    Med Clin (Barc); 1982 Sep 16; 79(5):227-31. PubMed ID: 6755088
    [No Abstract] [Full Text] [Related]

  • 13. [Two autopsy cases of adult-type acid maltase deficiency with vacuolation of cerebral arterial walls].
    Matsuoka Y, Hirayama M, Senda Y, Matsui T.
    Rinsho Shinkeigaku; 1985 Jan 16; 25(1):39-45. PubMed ID: 3922655
    [No Abstract] [Full Text] [Related]

  • 14. Late-onset acid maltase deficiency in a Chinese girl.
    Wong KS, Lai C, Ng HK.
    Clin Exp Neurol; 1991 Jan 16; 28():210-8. PubMed ID: 1821829
    [Abstract] [Full Text] [Related]

  • 15. [Myopathy caused by acid maltase deficiency in an adult].
    Cartier L, Cea JG, Slachevsky A.
    Rev Med Chil; 1995 Jun 16; 123(6):758-61. PubMed ID: 8525231
    [Abstract] [Full Text] [Related]

  • 16. [Late infantile form of Pompe's disease. Deficiency of alpha-1,4-glucosidase (acid maltase)].
    Colomer J, Roig M, Campistol J, Rullan G, Fernández-Alvarez E.
    An Esp Pediatr; 1984 Sep 15; 21(3):250-9. PubMed ID: 6391315
    [Abstract] [Full Text] [Related]

  • 17. Replacing acid alpha-glucosidase in Pompe disease: recombinant and transgenic enzymes are equipotent, but neither completely clears glycogen from type II muscle fibers.
    Raben N, Fukuda T, Gilbert AL, de Jong D, Thurberg BL, Mattaliano RJ, Meikle P, Hopwood JJ, Nagashima K, Nagaraju K, Plotz PH.
    Mol Ther; 2005 Jan 15; 11(1):48-56. PubMed ID: 15585405
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. [Glycogenosis caused by amylo-1,6-glucosidase deficiency. Myopathy as a lead finding in adults].
    Bröker HJ, Kuhn E, Fiehn W, Assmus H, Schröder JM.
    Schweiz Med Wochenschr; 1981 Jun 06; 111(23):854-8. PubMed ID: 6791275
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.